Canonical Allele Identifier: CA82750723

Gene: CD86

Linked Data

• dbSNP Id: rs888759228
• MyVariant Identifiers: chr3:g.121838333T>C (hg19) ; chr3:g.122119486T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122119486T>C , CM000665.2:g.122119486T>C	GRCh38
NC_000003.11:g.121838333T>C , CM000665.1:g.121838333T>C	GRCh37
NC_000003.10:g.123321023T>C	NCBI36
NG_029928.1:g.69125T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330540.7:c.942T>C MANE Select	ENSP00000332049.2:p.Phe314=
ENST00000264468.9:c.780T>C	ENSP00000264468.6:p.Phe260=
ENST00000330540.6:c.942T>C	ENSP00000332049.2:p.Phe314=
ENST00000393627.6:c.924T>C	ENSP00000377248.2:p.Phe308=
ENST00000469710.5:c.696T>C	ENSP00000418988.1:p.Phe232=
ENST00000478741.1:c.784T>C
ENST00000493101.5:c.606T>C	ENSP00000420230.1:p.Phe202=
NM_001206924.1:c.606T>C	NP_001193853.1:p.Phe202=
NM_001206925.1:c.696T>C	NP_001193854.1:p.Phe232=
NM_006889.4:c.924T>C	NP_008820.3:p.Phe308=
NM_175862.4:c.942T>C	NP_787058.4:p.Phe314=
NM_176892.1:c.780T>C	NP_795711.1:p.Phe260=
NM_175862.5:c.942T>C MANE Select	NP_787058.5:p.Phe314=
NM_001206924.2:c.606T>C	NP_001193853.2:p.Phe202=
NM_001206925.2:c.696T>C	NP_001193854.2:p.Phe232=
NM_006889.5:c.924T>C	NP_008820.4:p.Phe308=
NM_176892.2:c.780T>C	NP_795711.2:p.Phe260=